Canonical Allele Identifier: PA2573069551
Gene: RARB HGNC NCBI

Linked Data

ClinVar Variation Id: 1309156
ClinVar RCV Id: RCV001765325
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001277145.1:p.His298Pro
CA351886355
NM_001290216.3:c.893A>C
CA2573052133
NM_001290216.3:c.893_894delinsCA